GIMAP2 抗体 (AA 21-120)
Quick Overview for GIMAP2 抗体 (AA 21-120) (ABIN872766)
抗原
See all GIMAP2 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 21-120
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交叉反应
- 人
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human GIMAP2
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亚型
- IgG
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anti-GTPase, IMAP Family Member 2 (GIMAP2) antibody
GIMAP2 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 2 (GIMAP2) (AA 1-100) antibodyGIMAP2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1E10 unconjugated
anti-GTPase, IMAP Family Member 2 (GIMAP2) (AA 1-337) antibodyGIMAP2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 2 (GIMAP2) (AA 201-250) antibodyGIMAP2 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 2 (GIMAP2) (Internal Region) antibodyGIMAP2 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-GTPase, IMAP Family Member 2 (GIMAP2) (Middle Region) antibodyGIMAP2 适用: 人, Cow, 犬, 豚鼠, 马, 小鼠, Pig, 兔, 大鼠, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
other()
ICC 1:100-500 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- GIMAP2 (GTPase, IMAP Family Member 2 (GIMAP2))
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别名
- Gimap2
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背景
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Synonyms: GTPase, IMAP family member 2, HIMAP2, IMAP2, Immunity associated protein 2, GIMA2_HUMAN.
Background: The GTPase of the immunity-associated protein (GIMAP) family of proteins include seven members that are expressed by genes residing on human chromosome 7. GIMAP proteins have been implicated in the regulation of lymphomyeloid cell survival. GIMAP2 (GTPase IMAP family member 2), also known as IMAP2 (immunity-associated protein 2) or HIMAP2, is a 337 amino acid multi-pass membrane protein that is encoded by a gene located on human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
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基因ID
- 26157
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UniProt
- Q9UG22
抗原
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